06.-07.10.2021

Live Online Training: How to write the Quality Part of an IMPD

In this two days conference, Dr. Hiltrud Horn will give detailed insight into the Quality Part of an IMPD. Her presentations on the first day will cover regulatory requirements and challenges of the IMPD. She will provide guidance and advice on the planning, preparation and submission of the IMPD. On the second day you will learn how to efficiently write the Quality section of an IMPD. Furthermore she will present a case study about "Planning of an IMPD". Learn about the changing environment for clinical trials and get prepared for this now.

For more information please visit the following website:

(Conference organized by Concept Heidelberg)


Back

HOTLINE

Phone +49 (0) 7251/305 529
Fax +49 (0) 7251/305 528
Mail

Events

  • 18.-19.06.2024
    Online Seminar: Der Regulatory Affairs Manager
    More
Get all events



News

  • 19.12.2022
    EU Update regarding Deadlines of Nitrosamine Impurities
    More
  • 01.09.2022
    EU-GMP Annex 1 finally published
    More
  • 26.08.2022
    New Deadlines and Chances for Nitrosamines
    More
Get all news